Calcium imaging is a scientific technique usually carried out in research which is designed to show the calcium (Ca2+) status of a cell, tissue or medium. Calcium imaging techniques take advantage of so-called calcium indicators, fluorescent molecules that can respond to the binding of Ca2+ ions by changing their fluorescence properties. Two main classes of calcium indicators exist: chemical indicators and genetically encoded calcium indicators (GECI). Calcium imaging can be used to optically probe intracellular calcium in living animals. This technique has allowed studies of neuronal activity in hundreds of neurons and glial cells within neuronal circuits.
Chemical indicators are small molecules that can chelate calcium ions. All these molecules are based on an EGTA homologue called BAPTA, with high selectivity for calcium (Ca2+) ions versus magnesium (Mg2+) ions.
These dyes are generally used with the chelator carboxyl groups masked as acetoxymethyl esters, in order to render the molecule lipophilic and to allow easy entrance into the cell. Once the indicator is in the cell, cellular esterases will free the carboxyl and the indicator will be able to bind calcium. Binding of a Ca2+ ion to a fluorescent indicator molecule leads to either an increase in quantum yield of fluorescence or emission/excitation wavelength shift. Individual chemical Ca2+ fluorescent indicators were successfully utilized for cytosolic calcium measurements in a number of cellular preparations. Relative responses from a combination of chemical Ca2+ fluorescent indicators were also used to quantify calcium transients in intracellular organelles such as mitochondria.
Genetically encoded indicator
These indicators are fluorescent proteins derived from green fluorescent protein (GFP) or its variants (e.g. circularly permuted GFP, YFP, CFP), fused with calmodulin (CaM) and the M13 domain of the myosin light chain kinase, which is able to bind CaM.
Genetically encoded indicators do not need to be loaded onto cells, instead the genes encoding for these proteins can be easily transfected to cell lines. It is also possible to create transgenic animals expressing the dye in all cells or selectively in certain cellular subtypes.
Regardless of the type of indicator used the imaging procedure is generally very similar. Cells loaded with an indicator or expressing it in the case of GECI, can be viewed using a fluorescence microscope and captured by a CCD camera. Images are analyzed by measuring fluorescence intensity changes for a single wavelength or two wavelengths expressed as a ratio (ratiometric indicators). The derived fluorescence intensities and ratios are plotted against calibrated values for known Ca2+ levels to learn Ca2+ concentration.
- Stosiek, C, Garaschuk, O, Holthoff, K, Konnerth, A (2003). "In vivo two-photon calcium imaging of neuronal networks". Proceedings of the National Academy of Sciences 100 (12): 7319. doi:10.1073/pnas.1232232100.
- Ivannikov, M. et al. (2013). "Mitochondrial Free Ca2+ Levels and Their Effects on Energy Metabolism in Drosophila Motor Nerve Terminals". Biophys. J. 104 (11): 2353–2361. doi:10.1016/j.bpj.2013.03.064. PMC 3672877. PMID 23746507.
Nuccitelli, Richard (1994). A Practical guide to the study of calcium in living cells. Boston: Academic Press. ISBN 0-12-564141-9.
C. , Richard (1994). "A Practical guide to the study of calcium in living cells". Boston: Academic Press. ISBN 0-12-564141-9.